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三维环挤出。

Three-dimensional loop extrusion.

机构信息

University of Edinburgh, SUPA, School of Physics and Astronomy, Peter Guthrie Road, Edinburgh, UK.

University of Edinburgh, SUPA, School of Physics and Astronomy, Peter Guthrie Road, Edinburgh, UK; MRC Human Genetics Unit, Institute of Genetics and Cancer, University of Edinburgh, Edinburgh, UK.

出版信息

Biophys J. 2021 Dec 21;120(24):5544-5552. doi: 10.1016/j.bpj.2021.11.015. Epub 2021 Nov 15.

Abstract

Loop extrusion convincingly describes how certain structural maintenance of chromosome (SMC) proteins mediate the formation of large DNA loops. Yet most of the existing computational models cannot reconcile recent in vitro observations showing that condensins can traverse each other, bypass large roadblocks, and perform steps longer than their own size. To fill this gap, we propose a three-dimensional (3D) "trans-grabbing" model for loop extrusion, which not only reproduces the experimental features of loop extrusion by one SMC complex but also predicts the formation of so-called Z-loops via the interaction of two or more SMCs extruding along the same DNA substrate. By performing molecular dynamics simulations of this model, we discover that the experimentally observed asymmetry in the different types of Z-loops is a natural consequence of the DNA tethering in vitro. Intriguingly, our model predicts this bias to disappear in the absence of tethering and a third type of Z-loop, which has not yet been identified in experiments, to appear. Our model naturally explains roadblock bypassing and the appearance of steps larger than the SMC size as a consequence of non-contiguous DNA grabbing. Finally, this study is the first, to our knowledge, to address how Z-loops and bypassing might occur in a way that is broadly consistent with existing cis-only 1D loop extrusion models.

摘要

环挤压令人信服地描述了某些结构维持染色体 (SMC) 蛋白如何介导大 DNA 环的形成。然而,大多数现有的计算模型无法协调最近的体外观察结果,这些结果表明,凝聚素可以相互穿越,绕过大型障碍物,并进行比自身长度更长的步骤。为了填补这一空白,我们提出了一个三维(3D)的“跨抓取”环挤压模型,该模型不仅再现了一个 SMC 复合物的实验特征,还通过两个或更多 SMC 沿着相同的 DNA 底物挤压的相互作用,预测了所谓的 Z 环的形成。通过对该模型进行分子动力学模拟,我们发现实验中观察到的不同类型 Z 环的不对称性是体外 DNA 束缚的自然结果。有趣的是,我们的模型预测,在没有束缚和第三种尚未在实验中确定的 Z 环的情况下,这种偏差会消失。我们的模型自然地解释了非连续 DNA 抓取是如何导致障碍物绕过和出现大于 SMC 大小的步骤的。最后,这项研究是我们所知的第一个广泛符合现有顺式 1D 环挤压模型的方式来解决 Z 环和绕过问题的研究。

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